Mckesson Medical-Surgical recalls ClomiPHENE Citrate 50mg tablets due to temperature abuse risks. Affected products were distributed without clear lot numbers for specific customers.
cGMP deviations: Temperature abuse
Mckesson Medical-Surgical recalls ClomiPHENE Citrate 5:00mg tablets that may have been exposed to improper temperatures. This could affect the medication's safety and effectiveness for patients using prescription hormone therapy.
Temperature abuse during storage or handling could compromise the medication's stability. This may lead to ineffective or unsafe hormone therapy for patients using the product.
Prescription patients using ClomiPHENE Citrate 50mg tablets from Mckesson Medical-Surgical. Those with specific prescription orders that were distributed without clear lot numbers are most at risk.
Check for ClomiPHENE Citrate Tablets, USP 50 mg, 30-count bottles with NDC 49884-701-55. Products were distributed by Mckesson Medical-Surgical without specific lot numbers for individual customers.
Identify the product by checking the NDC code 49884-701-55 and the 30-count bottle size.
The recall does not specify if the product is safe; it indicates potential temperature abuse risks that could affect safety.
Check for ClomiPHENE Citrate Tablets, USP 50 mg, 30-count bottles with NDC 49884-701-55 distributed by Mckesson Medical-Surgical without specific lot numbers.
The recall does not provide specific action steps; you should check with your pharmacy or healthcare provider for guidance.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall D-1041-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall D-1041-2022 from Mckesson Medical-Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
